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FDG Synthesis
FDG Synthesis

... this step, the conversion of the stereochemical centre of precursor mannose into glucose takes place. The leaving group, triflate is converted to trifluorosulfonic acid (CF3SO2OH) which is removed at a later stage in the purification process. In the subsequent step, the protective acetyl ester group ...
FDG - ZAG Zyklotron AG
FDG - ZAG Zyklotron AG

... this step, the conversion of the stereochemical centre of precursor mannose into glucose takes place. The leaving group, triflate is converted to trifluorosulfonic acid (CF3SO2OH) which is removed at a later stage in the purification process. In the subsequent step, the protective acetyl ester group ...
RESET YOUR BODY CORE BOOST // CLEANSE
RESET YOUR BODY CORE BOOST // CLEANSE

...  ilk Thistle extract - Native to Mediterranean regions, milk thistle seeds contain an antioxidant flavonoid complex that stimulates liver enzymes. It is also known to relieve digestive disturbances or indigestion. • Senna extract - Senna is a flowering plant that is used as natural herbal laxative ...
Acetic anhydride Product Number A6404 Store at - Sigma
Acetic anhydride Product Number A6404 Store at - Sigma

Core Section II: Frequent Symptoms Associated with Imminent
Core Section II: Frequent Symptoms Associated with Imminent

... Incontinence Decreased intake Core ...
Advanced Chemistry
Advanced Chemistry

... C. R1, R2 and R3 represent different sites for anchoring substituents. The class B was found to be active after screening. After routine manipulations utilizing the sites R1, R2 and R3, the compound C was established to be the most active and is eventually approved by the authority to be marketed as ...
Advanced Chemistry
Advanced Chemistry

... 4.A drug discovery program resulted in the three classes of compounds (Step 1) -- A, B and C. R1, R2 and R3 represent different sites for anchoring substituents. The class B was found to be active after screening. After routine manipulations utilizing the sites R 1, R2 and R3, the compound C was est ...
1

Kedarcidin



Kedarcidin is a chromoprotein antitumor antibiotic first isolated from an Actinomycete in 1992, comprising an ansa-bridged enediyne chromophore (shown) as well as an apoprotein that serves to stabilize the toxin in the Actinomycete. Like other members of the enediyne class of drugs - so named for the nine-or-ten-membered core structure bearing an alkene directly attached to two alkynyl appendages—kedarcidin was likely evolved to kill bacteria that compete with the producing organism. Because it achieves this by causing DNA damage, however, kedarcidin is capable of harming tumor cells, as well. Kedarcidin is thus the subject of scientific research, both for its structural complexity as well as its anticancer properties.
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